Lamb Jillian, Purdy Kerri, Sutherland Ashley
Division of Clinical Dermatology and Cutaneous Science, Department of Medicine, Dalhousie University, Halifax, NS, Canada.
SAGE Open Med Case Rep. 2024 Aug 22;12:2050313X241274855. doi: 10.1177/2050313X241274855. eCollection 2024.
Bullous pemphigoid is an autoimmune blistering disease affecting the dermo-epidermal junction, most commonly seen in older patients. First-line treatment includes systemic, topical corticosteroids and/or steroid-sparing immunosuppressants. Treatment with these medications may be limited by their safety profile. Dupilumab is a humanized monoclonal antibody targeting interleukin-4 and interleukin-13 cytokines currently indicated for moderate-to-severe atopic dermatitis, severe asthma, chronic rhinosinusitis with nasal polyposis, and moderate-to-severe prurigo nodularis. We report a case of a patient with recalcitrant bullous pemphigoid effectively treated with dupilumab.
大疱性类天疱疮是一种影响真皮-表皮交界处的自身免疫性水疱病,最常见于老年患者。一线治疗包括全身性、局部用皮质类固醇和/或糖皮质激素节省免疫抑制剂。这些药物的治疗可能会受到其安全性的限制。度普利尤单抗是一种靶向白细胞介素-4和白细胞介素-13细胞因子的人源化单克隆抗体,目前适用于中度至重度特应性皮炎、重度哮喘、伴有鼻息肉的慢性鼻-鼻窦炎以及中度至重度结节性痒疹。我们报告了一例用度普利尤单抗有效治疗的顽固性大疱性类天疱疮患者。